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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1390361Generated: October 27, 2026

Methanol → 1-N-methyl-4-nitrobenzene-1,2-diamine

https://huagongshe.com/reaction/1390361

Reaction equation

Participants

RoleNameHCIDCharge
ReactantMethanolHCID 887—
ReactantSodium SulfideHCID 14804—
ReactantN-methyl-2,4-dinitroanilineHCID 74891—
ReactantSodium BicarbonateHCID 516892—
SolventWaterHCID 962—
SolventSodium HydroxideHCID 14798—
Product1-N-methyl-4-nitrobenzene-1,2-diamineHCID 342002594.4%

Reaction Conditions

Temperature25 °C

Reaction Steps

71 Parts of 2,4-dinitro-N-methylaniline and 53 parts of sodium hydrogen carbonate are stirred in 144 parts of methanol. The yellow suspension is heated in the course of 20 minutes to 40° C. Simultaneously, 81.9 parts of 60% sodium sulphide are dissolved in 144 parts of water of approx. 40° C and 1.2 parts of 30% sodium hydroxide solution are added to the resultant solution. The turbid yellow solution is filtered. The clear yellow filtrate is added dropwise in the course of 2 hours to the suspension of 2,4-dinitro-N-methylaniline. An exothermic reaction occurs during the dropwise addition. The contents of the flask turn dark in colour. The new suspension is heated in the course of 1 hour to 70° C and stirred for 15 minutes at this temperature (reflux). Then 144 parts of methanol are distilled off. The residue is cooled to 25° C and 50 parts of ice are added. After suction filtration at 8° C, the filter cake is washed three times with 160 parts of water and dried in vacuo at 60° C, affording 56.8 parts of 2-amino-4-nitro-N-methylaniline (94.4% of theory). The melting point of the product is 177°-178° C.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS04138568
Source datasetuspto-grants-1979_02
ORD IDord-d7f27637653a41e0a1945b969a420bb7
Source noteuspto-grants-1979_02